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<article article-type="research-article" dtd-version="1.3" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xml:lang="ru"><front><journal-meta><journal-id journal-id-type="publisher-id">zhps</journal-id><journal-title-group><journal-title xml:lang="ru">Журнал прикладной спектроскопии</journal-title><trans-title-group xml:lang="en"><trans-title>Zhurnal Prikladnoii Spektroskopii</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">0514-7506</issn><publisher><publisher-name>B. I. Stepanov Institute of Physics of the National Academy of Sciences</publisher-name></publisher></journal-meta><article-meta><article-id custom-type="elpub" pub-id-type="custom">zhps-572</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>Статьи</subject></subj-group></article-categories><title-group><article-title>МЕХАНИЗМ АННИГИЛЯЦИОННОЙ ЗАМЕДЛЕННОЙ ФЛУОРЕСЦЕНЦИИ РАСТВОРА 7-АЗАИНДОЛА В ЦИКЛОГЕКСАНЕ</article-title><trans-title-group xml:lang="en"><trans-title>MECHANISM OF THE ANNIHILATION DELAYED FLUORESCENCE OF 7-AZAINDOLE SOLUTION IN CYCLOHEXANE</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Суходола</surname><given-names>А. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Sukhodola</surname><given-names>A. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>220072, Минск, просп. Независимости, 68-2</p></bio><bio xml:lang="en"><p>68-2 Nezavisimosti Prosp., Minsk, 220072</p></bio><email xlink:type="simple">sukhodola@imaph.bas-net.by</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Институт физики НАН Беларуси</institution></aff><aff xml:lang="en"><institution>B. I. Stepanov Institute of Physics of the National Academy of Sciences of Belarus</institution></aff></aff-alternatives><pub-date pub-type="collection"><year>2019</year></pub-date><pub-date pub-type="epub"><day>20</day><month>03</month><year>2020</year></pub-date><volume>86</volume><issue>3</issue><fpage>360</fpage><lpage>367</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Суходола А.А., 2020</copyright-statement><copyright-year>2020</copyright-year><copyright-holder xml:lang="ru">Суходола А.А.</copyright-holder><copyright-holder xml:lang="en">Sukhodola A.A.</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://zhps.ejournal.by/jour/article/view/572">https://zhps.ejournal.by/jour/article/view/572</self-uri><abstract/><trans-abstract xml:lang="en"><p>The spectral-kinetic characteristics of the annihilation delayed fluorescence (ADF) of 7-azaindole solution in cyclohexane were measured at room temperature. Two bands with maxima at 345 and 480 nm were observed in the ADF spectrum. The short-wavelength band is interpreted as ADF of dimers formed due to dipole-dipole interactions of molecules in excited singlet and ground states, which are populated as a result of triplet-triplet annihilation of monomers. The long-wavelength band refers to the ADF of dimertautomers, which are formed due to the double hydrogen bond and double proton transfer. Excited singlet states of dimers-tautomers are populated as a result of the mixed annihilation of the triplet states of monomers and dimers-tautomers. The decay kinetics of triplet states of monomers and dimers-tautomers is determined mainly by triplet-triplet annihilation processes.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>7-азаиндол</kwd><kwd>димер</kwd><kwd>спектр поглощения</kwd><kwd>флуоресценция</kwd><kwd>аннигиляционная замедленная флуоресценция</kwd><kwd>триплетные состояния</kwd><kwd>кинетика длительной люминесценции</kwd></kwd-group><kwd-group xml:lang="en"><kwd>7-azaindole</kwd><kwd>dimer</kwd><kwd>annihilation delayed fluorescence</kwd><kwd>triplet states</kwd><kwd>kinetic of long-lasting luminescence</kwd></kwd-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">М. Negrerie, F. Gai, J.-C. Lambry, J.-L. Martin, W.J. Petrich. J. Phys. Chem., 97 (1993) 5046—5049</mixed-citation><mixed-citation xml:lang="en">М. Negrerie, F. Gai, J.-C. Lambry, J.-L. Martin, W.J. Petrich. J. Phys. 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